Tamsulosin Hydrochloride
- Product NDC
- 63629-8135
- 11-digit product format
- 636298135
- Labeler code
- 63629
- Product ID
- 63629-8135_469cc978-ab5f-4957-bfe6-f28beecc5ee9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202433
- Marketing category
- ANDA
- Marketing start
- 2013-04-30
- Marketing end
- 0000-00-00
- Substance
- TAMSULOSIN HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 11SV1951MR | TAMSULOSIN HYDROCHLORIDE | 106463-17-6 | TAMSULOSIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8135-1 | 63629813501 | 30 CAPSULE in 1 BOTTLE (63629-8135-1) | 30 capsule | 2019-07-15 | 0000-00-00 | No | No | Current |
| 63629-8135-2 | 63629813502 | 90 CAPSULE in 1 BOTTLE (63629-8135-2) | 90 capsule | 2019-07-15 | 0000-00-00 | No | No | Current |